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艾美耳球虫蛋白酶,一种组织蛋白酶 B 样半胱氨酸蛋白酶,在艾美耳属寄生虫的孢子形成过程中表达。

Eimeripain, a cathepsin B-like cysteine protease, expressed throughout sporulation of the apicomplexan parasite Eimeria tenella.

机构信息

INRA, UMR1282, Equipe Pathogenèse des Coccidioses, Infectiologie et Santé Publique, Nouzilly, France.

出版信息

PLoS One. 2012;7(3):e31914. doi: 10.1371/journal.pone.0031914. Epub 2012 Mar 22.

Abstract

The invasion and replication of Eimeria tenella in the chicken intestine is responsible for avian coccidiosis, a disease that has major economic impacts on poultry industries worldwide. E. tenella is transmitted to naïve animals via shed unsporulated oocysts that need contact with air and humidity to form the infectious sporulated oocysts, which contain the first invasive form of the parasite, the sporozoite. Cysteine proteases (CPs) are major virulence factors expressed by protozoa. In this study, we show that E. tenella expresses five transcriptionally regulated genes encoding one cathepsin L, one cathepsin B and three cathepsin Cs. Biot-LC-LVG-CHN₂, a cystatin derived probe, tagged eight polypeptides in unsporulated oocysts but only one in sporulated oocysts. CP-dependant activities were found against the fluorescent substrates, Z-FR-AMC and Z-LR-AMC, throughout the sporulation process. These activities corresponded to a cathepsin B-like enzyme since they were inhibited by CA-074, a specific cathepsin B inhibitor. A 3D model of the catalytic domain of the cathepsin B-like protease, based on its sequence homology with human cathepsin B, further confirmed its classification as a papain-like protease with similar characteristics to toxopain-1 from the related apicomplexan parasite, Toxoplasma gondii; we have, therefore, named the E. tenella cathepsin B, eimeripain. Following stable transfection of E. tenella sporozoites with a plasmid allowing the expression of eimeripain fused to the fluorescent protein mCherry, we demonstrated that eimeripain is detected throughout sporulation and has a punctate distribution in the bodies of extra- and intracellular parasites. Furthermore, CA-074 Me, the membrane-permeable derivative of CA-074, impairs invasion of epithelial MDBK cells by E. tenella sporozoites. This study represents the first characterization of CPs expressed by a parasite from the Eimeria genus. Moreover, it emphasizes the role of CPs in transmission and dissemination of exogenous stages of apicomplexan parasites.

摘要

柔嫩艾美耳球虫在鸡肠道中的侵袭和复制是引起禽球虫病的原因,该病对全球家禽业造成了重大的经济影响。柔嫩艾美耳球虫通过脱落未孢子化的卵囊传播给幼稚动物,这些卵囊需要接触空气和湿度才能形成传染性孢子化卵囊,其中包含寄生虫的第一个侵袭形式,即孢子。半胱氨酸蛋白酶(CPs)是原生动物表达的主要毒力因子。在这项研究中,我们表明柔嫩艾美耳球虫表达了五个转录调节基因,编码一个组织蛋白酶 L、一个组织蛋白酶 B 和三个组织蛋白酶 C。生物素-LC-LVG-CHN₂,一种衍生自半胱氨酸蛋白酶抑制剂的探针,在未孢子化卵囊中标记了 8 条多肽,但在孢子化卵囊中只标记了 1 条。在整个孢子形成过程中,在荧光底物 Z-FR-AMC 和 Z-LR-AMC 上都发现了 CP 依赖性活性。这些活性与组织蛋白酶 B 样酶相对应,因为它们被特定的组织蛋白酶 B 抑制剂 CA-074 抑制。基于其与人类组织蛋白酶 B 的序列同源性,对组织蛋白酶 B 样蛋白酶的催化结构域进行了 3D 建模,进一步证实了其分类为木瓜蛋白酶样蛋白酶,与相关的顶复门寄生虫弓形虫中的 toxopain-1 具有相似的特征;因此,我们将柔嫩艾美耳球虫的组织蛋白酶 B 命名为 eimeripain。在稳定转染表达与荧光蛋白 mCherry 融合的 eimeripain 的柔嫩艾美耳球虫孢子后,我们证明 eimeripain 在整个孢子形成过程中被检测到,并在体外和体内寄生虫的体中呈点状分布。此外,CA-074 Me,CA-074 的膜通透衍生物,可损害柔嫩艾美耳球虫孢子对上皮 MDBK 细胞的侵袭。这项研究代表了对艾美耳球虫属寄生虫表达的 CPs 的首次表征。此外,它强调了 CPs 在顶复门寄生虫外源阶段的传播和传播中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c53/3310820/736d4a49475b/pone.0031914.g001.jpg

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